Search research articles
Contact Us
Filters
Showing results (41-50 of 154) with videos related to
Page
of 16
Sort By:
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies
|
July 1, 1994
Tissue kallikrein activity and kinin release in human endothelial cells
K Graf, M Gräfe, W Auch-Schwelk, et al.
Human Genetics
|
May 1, 1995
Number and sex of offspring of delta F508 carriers outside cystic fibrosis families
H G de Vries, J M Collée, W P Meeuwsen, et al.
Nucleic Acids Research
|
January 12, 1987
A high frequency RFLP identified by an anonymous single copy genomic clone at 13q14.1-13q14.2 [HGM8 assignment no. D13S22]
A M Bowcock, H Scheffer, J M Hebert, et al.
Prenatal Diagnosis
|
September 1, 1992
Prenatal diagnosis in a family with X-linked chronic granulomatous disease with the use of the polymerase chain reaction
M De Boer, B G Bolscher, R H Sijmons, et al.
The American Journal of Gastroenterology
|
August 10, 2005
Impaired bolus transit across the esophagogastric junction in postfundoplication dysphagia
R C H Scheffer, M Samsom, A Haverkamp, et al.
Human Mutation
|
January 1, 1996
Comprehensive and accurate mutation scanning of the CFTR gene by two-dimensional DNA electrophoresis
Y Wu, R M Hofstra, H Scheffer, et al.
The British Journal of Surgery
|
September 24, 2004
Long-term effect of fundoplication on motility of the oesophagus and oesophagogastric junction
R C H Scheffer, M Samsom, T G Frakking, et al.
Cancer Research
|
December 1, 1992
Analysis of a metastasizing testicular mixed gonadal stromal tumor with osteosarcoma components suggests that a malignant tumor with the histology of osteosarcoma may develop without primary involvement of RB1 and TP53
P T Reuvekamp, R P Stulp, H Schraffordt Koops, et al.
Human Genetics
|
December 1, 1987
Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease
H Scheffer, I P Kema, I Kondo, et al.
American Journal of Human Genetics
|
October 1, 1995
Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy
J M Cobben, G van der Steege, P Grootscholten, et al.
Page
of 16
Search research articles
Search
Showing results (41-50 of 154) with videos related to
Sort By:
Page
of 16
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies
|
July 1, 1994
Tissue kallikrein activity and kinin release in human endothelial cells
K Graf, M Gräfe, W Auch-Schwelk, et al.
Human Genetics
|
May 1, 1995
Number and sex of offspring of delta F508 carriers outside cystic fibrosis families
H G de Vries, J M Collée, W P Meeuwsen, et al.
Nucleic Acids Research
|
January 12, 1987
A high frequency RFLP identified by an anonymous single copy genomic clone at 13q14.1-13q14.2 [HGM8 assignment no. D13S22]
A M Bowcock, H Scheffer, J M Hebert, et al.
Prenatal Diagnosis
|
September 1, 1992
Prenatal diagnosis in a family with X-linked chronic granulomatous disease with the use of the polymerase chain reaction
M De Boer, B G Bolscher, R H Sijmons, et al.
The American Journal of Gastroenterology
|
August 10, 2005
Impaired bolus transit across the esophagogastric junction in postfundoplication dysphagia
R C H Scheffer, M Samsom, A Haverkamp, et al.
Human Mutation
|
January 1, 1996
Comprehensive and accurate mutation scanning of the CFTR gene by two-dimensional DNA electrophoresis
Y Wu, R M Hofstra, H Scheffer, et al.
The British Journal of Surgery
|
September 24, 2004
Long-term effect of fundoplication on motility of the oesophagus and oesophagogastric junction
R C H Scheffer, M Samsom, T G Frakking, et al.
Cancer Research
|
December 1, 1992
Analysis of a metastasizing testicular mixed gonadal stromal tumor with osteosarcoma components suggests that a malignant tumor with the histology of osteosarcoma may develop without primary involvement of RB1 and TP53
P T Reuvekamp, R P Stulp, H Schraffordt Koops, et al.
Human Genetics
|
December 1, 1987
Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease
H Scheffer, I P Kema, I Kondo, et al.
American Journal of Human Genetics
|
October 1, 1995
Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy
J M Cobben, G van der Steege, P Grootscholten, et al.
Page
of 16